Replication of tcf4 through association and linkage studies in late-onset fuchs endothelial corneal dystrophy

• Main Authors: Li Y.-J., Minear M.A., Rimmler J., Zhao B., Balajonda E., Hauser M.A., Allingham R.R., Eghrari A.O., Riazuddin S.A., Katsanis N., Gottsch J.D., Gregory S.G., Klintworth G.K., Afshari N.A.
• 其他作者: DUKE-NUS MEDICAL SCHOOL
• 格式: Article
• 出版: 2019
• 主題: protein TCF4; T cell factor protein; unclassified drug; basic helix loop helix leucine zipper transcription factor; TCF4 protein, human; transcription factor; adult; allele; article; chromosome 18; congenital cornea dystrophy; controlled study; dominant gene; family history; female; gene frequency; gene function; gene location; gene replication; gene targeting; genetic association; genetic linkage; genetic model; genetic predisposition; genetic variability; genotype; heterozygote; human; male; marker gene; onset age; pathogenesis; recessive gene; scoring system; single nucleotide polymorphism; validation process; biological model; genetic marker; genetics; intron; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Chromosomes, Human, Pair 18; Fuchs' Endothelial Dystrophy; Genetic Linkage; Genetic Markers; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Introns; Models, Genetic; Polymorphism, Single Nucleotide; Transcription Factors
• 在線閱讀: https://scholarbank.nus.edu.sg/handle/10635/162053

10.1371/journal.pone.0018044